Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678723Generated: October 31, 2026

Triphenylphosphine → HCID 59373762, compound

https://huagongshe.com/reaction/1678723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiamideHCID 5353800—
ReactantHCID 59370765HCID 59370765—
ReactantHCID 67330214HCID 67330214—
SolventTolueneHCID 1140—
ProductHCID 59373762HCID 59373762—

Reaction Steps

Tert-butyl 3-ethyl-6-hydroxyindazole-1-carboxylate (27.9 mg) that can be produced by the method described in Reference Example 14 or the like, and a (R)-tert-butyl 5-(2-(benzyl(2-hydroxyethyl)amino)-1-(triethylsilyloxy)ethyl)-2-chlorophenyl(methylsulfonyl)carbamate-toluene solution [0.5 mL; solution prepared by dissolving (R)-tert-butyl 5-(2-(benzyl(2-hydroxyethyl)amino)-1-(triethylsilyloxy)ethyl)-2-chlorophenyl(methylsulfonyl)carbamate (1.5265 g) that can be produced by the method described in Reference Example 75 or the like in dehydrated toluene (10 mL)] were dissolved in dehydrated toluene (0.5 mL), and triphenylphosphine (54.9 mg; manufactured by Wako Pure Chemical Industries, Ltd.) and TMAD (41.4 mg; manufactured by Masuda Chemical Industries, Co., Ltd.) were added to the solution. The mixture was stirred for 3 days at room temperature. The reaction solution was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=85:15→64:36), and thus the title compound (85.6 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008506B2
Source datasetuspto-grants-2011_08
ORD IDord-2140ce4f59da4b55b5427189ae094db0
Source noteuspto-grants-2011_08